713-65-5

  • Product Name:1-Nitro-4-(trifluoromethoxy)benzene
  • Molecular Formula:C7H4F3NO3
  • Purity:99%
  • Molecular Weight:207.109
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Product Details;

CasNo: 713-65-5

Molecular Formula: C7H4F3NO3

factory and supplier 713-65-5 1-Nitro-4-(trifluoromethoxy)benzene in stock

  • Molecular Formula:C7H4F3NO3
  • Molecular Weight:207.109
  • Vapor Pressure:0.196mmHg at 25°C 
  • Melting Point:15°C 
  • Refractive Index:1.467 
  • Boiling Point:217.4 °C at 760 mmHg 
  • Flash Point:85.3 °C 
  • PSA:55.05000 
  • Density:1.461 g/cm3 
  • LogP:3.01660 

4-(Trifluoromethoxy)nitrobenzene(Cas 713-65-5) Usage

InChI:InChI=1/C7H4F3NO3/c8-7(9,10)14-6-3-1-5(2-4-6)11(12)13/h1-4H

713-65-5 Relevant articles

Method for synthesizing nitro (hetero) aromatic hydrocarbon

-

Paragraph 0082-0084; 0085-0087, (2022/04/08)

The invention discloses a method for syn...

Electrochemical Trifluoromethoxylation of (Hetero)aromatics with a Trifluoromethyl Source and Oxygen

Ouyang, Yao,Qing, Feng-Ling,Xu, Xiu-Hua

supporting information, (2021/12/06)

Trifluoromethoxylated aromatics (ArOCF3)...

Radical C?H Trifluoromethoxylation of (Hetero)arenes with Bis(trifluoromethyl)peroxide

Dix, Stefan,Golz, Paul,Schmid, Jonas R.,Riedel, Sebastian,Hopkinson, Matthew N.

supporting information, p. 11554 - 11558 (2021/07/09)

Trifluoromethoxylated (hetero)arenes are...

NITRATION

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Page/Page column 36; 38; 42; 52; 66, (2020/05/28)

The present invention relates to a proce...

713-65-5 Process route

1-trifluoromethoxybenzene
456-55-3

1-trifluoromethoxybenzene

4-nitrophenyl trifluoromethyl ether
713-65-5

4-nitrophenyl trifluoromethyl ether

o-nitro-α,α,α-trifluoromethoxybenzene
1644-88-8

o-nitro-α,α,α-trifluoromethoxybenzene

Conditions
Conditions Yield
With magnesium(II) perchlorate; 2-nitrobenzo[d]isothiazol-3(2H)-one 1,1-dioxide; In [D3]acetonitrile; at 85 ℃; for 19h; Overall yield = 97 percent; Inert atmosphere; Sealed tube;
79.7%
17.3%
With nitronium tetrafluoborate; In nitromethane; at 25 ℃; for 2h; Product distribution; further nitrating reagents, solvents and temperature; investigation of the nitration reaction; Hammett-Brown plot (relative reactivity data compared to benzene);
11.5 % Chromat.
88.5 % Chromat.
With sulfuric acid; nitric acid; at -0.16 ℃; Temperature; Flow reactor;
90.97 %Chromat.
7.26 %Chromat.
3-methyl-4-nitro-1-(trifluoromethoxy)-6-(trifluoromethyl)-1H-benzo[d][1,2,3]triazol-3-ium trifluoromethanesulfonate

3-methyl-4-nitro-1-(trifluoromethoxy)-6-(trifluoromethyl)-1H-benzo[d][1,2,3]triazol-3-ium trifluoromethanesulfonate

nitrobenzene
98-95-3,26969-40-4

nitrobenzene

4-nitrophenyl trifluoromethyl ether
713-65-5

4-nitrophenyl trifluoromethyl ether

1-nitro-3-(trifluoromethoxy)benzene
2995-45-1

1-nitro-3-(trifluoromethoxy)benzene

o-nitro-α,α,α-trifluoromethoxybenzene
1644-88-8

o-nitro-α,α,α-trifluoromethoxybenzene

Conditions
Conditions Yield
With tris(2,2-bipyridine)ruthenium(II) hexafluorophosphate; In acetonitrile; at 20 ℃; for 1h; Overall yield = 40 percentSpectr.; Inert atmosphere; Flow reactor; Irradiation;

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